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Wire, Orthodontic

FDA product code DZC · Class 1 · Dental

42,797
Registered devices
328
Adverse events
4
Recalls
30
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2015-11-04Ormco/SybronendoOrmco Corporation is recalling Copper NiTi Preformed Archwires because the product transformation temperature as listed on the labeling is incorrect.
2013-12-13Highland Metals, Inc.Labeling issue: Product labeled as "Upper" may contain "Lower" archwires with a red midline mark. Product labeled ad "Lower" may contain "Upper" archwires with
2013-12-13Highland Metals, Inc.Labeling issue: Product labeled as "Upper" may contain "Lower" archwires with a red midline mark. Product labeled ad "Lower" may contain "Upper" archwires with
2011-03-15Ormco CorporationThe TMA Lower Broad Arch packages labeled with part number 211-1402 actually contained TMA Upper Archwires, part number 2021007.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.